Jobs · Analyst · Texas

Associate Clinical Trial Manager - PhD - Postdoctoral - Infectious Diseases - Dallas

Medpace · Irving, TX · 2 wk ago
On-siteAnalystFull-time

About the Role

Medpace is seeking candidates with PhDs and/or Post-Doctoral Research experience related to Infectious Disease areas for a full-time, office-based Associate Clinical Trial Manager (aCTM) position in Dallas, TX. This role offers a fantastic opportunity for recent PhD graduates to transition into the industry, receive solid foundational training, and develop a career in the research and development of cutting-edge therapeutics. Candidates should expect an intensive training period and demonstrate the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

Responsibilities

  • Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
  • Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
  • Compile and maintain project-specific status reports within the clinical trial management system
  • Interact with the internal project team, Sponsor, study sites, and third-party vendors
  • Provide oversight and quality control of our internal regulatory filing system
  • Provide oversight and management of study supplies
  • Create and maintain project timelines
  • Coordinate project meetings and produce quality minutes

Qualifications

  • PhD in Life Sciences
  • Expertise related to Infectious Diseases
  • Ability to work in a fast-paced dynamic industry within an international team
  • Prior experience within the CRO or pharmaceutical industry not required but will be advantageous

About Medpace

Medpace is a full-service clinical contract research organization (CRO) providing phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs more than 6,500 people across 40+ countries.

Why Medpace?

  • Purpose-Driven Work: Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence.
  • Collaborative Culture: Contribute to an interactive team environment that empowers decision-making, creative thinking, and continuous learning through open communication and mutual trust. Leadership is both accessible and approachable.
  • Continuous Growth & Development:
    • Office-based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry-renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Benefits

  • Competitive compensation programs that recognize and reward performance
  • Comprehensive health, wellness, retirement, and PTO benefits
  • Office-based culture with occasional work-from-home flexibility for eligible positions after training
  • Company-sponsored social events

Please note benefits may vary based on country.

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